Atlas FDA

Rapid fFN for the TLiIQ System

FDA premarket approval P920048/S022 · decided 2022-04-13

Approval details

PMA number
P920048
Supplement
S022
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Rapid fFN for the TLiIQ System
Generic name
ENZYME IMMUNOASSAY, FETAL FIBRONECTIN
Applicant
Hologic, Inc.
Date received
2022-03-31
Decision date
2022-04-13
Days to decision
13 days
Decision code
OK30
Product code
LKV
Advisory committee
Clinical Toxicology
Expedited review
No
Location
Sunnyvale, CA
Statement
Change in incoming release criteria for the nitrocellulose component of the Rapid fFN for the TLiIQ System.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
CoolSeal Generator® (CSL-200-90) (K253634)Hologic, Inc.2026-06-17
Panther Fusion GI Expanded Bacterial Assay (K251993)Hologic, Inc.2025-09-25
Genius AI Detection 2.0 (K243341)Hologic, Inc.2025-07-31
Aptima SARS-CoV-2 Assay (K243396)Hologic, Inc.2025-02-13
Aptima CMV Quant Assay (K243935)Hologic, Inc.2025-01-17
Aptima BV Assay; Aptima CV/TV Assay (K243345)Hologic, Inc.2024-11-25
Panther Fusion SARS-CoV-2/Flu A/B/RSV assay (K242465)Hologic, Inc.2024-11-15
Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap Multipack (10-pack) (FLT-210); Fluent Pro Fluid Management System Waste Bag Multipack (5-pack) (FLT-205) (K240886)Hologic, Inc.2024-07-25